The Global Medical Device Testing And Certification Market is estimated to be valued at US$ 10,957.9 Mn in 2025 and is expected to exhibit a CAGR of 4.3% over the forecast period 2025 to 2032.

Medical device testing and certification involves rigorous evaluation of medical equipment, instruments, and systems to ensure safety, efficacy, and regulatory compliance before market entry. These services cover biocompatibility testing, electrical safety assessments, performance validation, and risk management procedures. Manufacturers increasingly rely on accredited laboratories for product quality verification, reducing time-to-market and minimizing recall risks.

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